Acetic Anhydride → Ethyl 2-(2-chloro-4,5-difluorobenzoyl)-3-ethoxyacrylate
반응식
[CH2:1]([O:3][C:4](=[O:17])[C:5](=O)[CH2:6][C:7]1[CH:12]=[C:11]([F:13])[C:10]([F:14])=[CH:9][C:8]=1[Cl:15])[CH3:2].[CH2:18]([O:20][CH:21](OCC)OCC)[CH3:19].C(OC(=O)C)(=[O:30])C>>[CH2:1]([O:3][C:4](=[O:17])[C:5]([C:6](=[O:30])[C:7]1[CH:12]=[C:11]([F:13])[C:10]([F:14])=[CH:9][C:8]=1[Cl:15])=[CH:21][O:20][CH2:18][CH3:19])[CH3:2]참가 물질
4
실험 절차
2-Chloro-4,5-difluoro-α-oxo-benzenepropanoic acid ethyl ester (20 g, 76 mmol), triethylorthoformate (17.0 g, 115 mmol) and acetic anhydride (19.5 g, 191 mmol) were combined and heated to reflux for 3 hours. Excess solvent was removed in vacuo to provide the crude title product, which was used without purification.
후처리
- temperatureheated
- temperatureto reflux for 3 hours
- customExcess solvent was removed in vacuo
출처 및 근거
- ORD 기록
- ord-10556f09c0af49d788866943a334d7bd
- 출처 데이터셋
- uspto-grants-1991_08
- 특허 번호
- US05037834
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